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IL TOTAL PROTEIN REAGENT

K802310 Class II Traditional
Decision Date
1980-10-23
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K802310
Product Code CEK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1635
Decision Date 1980-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IL TOTAL PROTEIN REAGENT received FDA 510(k) clearance under submission number K802310, sponsored by Instrumentation Laboratory CO. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1980-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code CEK and 21 CFR 862.1635, within the Clinical Chemistry review panel as a Class II device.